Canonical Allele Identifier: CA1538676706

Gene: AGXT2

Genomic Alleles

HGVS	Genome Assembly
NC_000005.10:g.34998768_34998771delinsTCTA , CM000667.2:g.34998768_34998771delinsTCTA	GRCh38
NC_000005.9:g.34998873_34998876delinsTCTA , CM000667.1:g.34998873_34998876delinsTCTA	GRCh37
NC_000005.8:g.35034630_35034633delinsTCTA	NCBI36

Transcript Alleles

HGVS	Amino-acid Change
ENST00000231420.11:c.1493_1496delinsTAGA MANE Select	ENSP00000231420.6:p.Val498=
ENST00000231420.10:c.1493_1496delinsTAGA	ENSP00000231420.6:p.Val498=
ENST00000510428.1:c.1268_1271delinsTAGA	ENSP00000422799.1:p.Val423=
ENST00000512135.5:n.1163_1166delinsTAGA
ENST00000618015.4:c.1268_1271delinsTAGA	ENSP00000479154.1:p.Val423=
NM_001306173.1:c.1268_1271delinsTAGA	NP_001293102.1:p.Val423=
NM_031900.3:c.1493_1496delinsTAGA	NP_114106.1:p.Val498=
XM_005248337.2:c.1490_1493delinsTAGA	XP_005248394.1:p.Val497=
XM_005248338.2:c.1298_1301delinsTAGA	XP_005248395.1:p.Val433=
XM_011514077.1:c.1438-369_1438-366delinsTAGA	XP_011512379.1:n.1438-369_1438-366delinsTAGA
XM_005248337.3:c.1490_1493delinsTAGA	XP_005248394.1:p.Val497=
XM_005248338.3:c.1298_1301delinsTAGA	XP_005248395.1:p.Val433=
XM_017009748.2:c.1268_1271delinsTAGA	XP_016865237.1:p.Val423=
NM_031900.4:c.1493_1496delinsTAGA MANE Select	NP_114106.1:p.Val498=
NM_001306173.2:c.1268_1271delinsTAGA	NP_001293102.1:p.Val423=